索引
生物
遗传学
放大器
基因分型
单核苷酸多态性
遗传标记
SNP基因分型
多路复用
基因座(遗传学)
分子反转探针
数量性状位点
基因型
DNA测序
离子半导体测序
SNP公司
标记辅助选择
计算生物学
聚合酶链反应
基因
作者
Amy Bernardo,Shan Wang,Paul St. Amand,Guihua Bai
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2015-12-01
卷期号:10 (12): e0143890-e0143890
被引量:37
标识
DOI:10.1371/journal.pone.0143890
摘要
With the advent of next generation sequencing (NGS) technologies, single nucleotide polymorphisms (SNPs) have become the major type of marker for genotyping in many crops. However, the availability of SNP markers for important traits of bread wheat (Triticum aestivum L.) that can be effectively used in marker-assisted selection (MAS) is still limited and SNP assays for MAS are usually uniplex. A shift from uniplex to multiplex assays will allow the simultaneous analysis of multiple markers and increase MAS efficiency. We designed 33 locus-specific markers from SNP or indel-based marker sequences that linked to 20 different quantitative trait loci (QTL) or genes of agronomic importance in wheat and analyzed the amplicon sequences using an Ion Torrent Proton Sequencer and a custom allele detection pipeline to determine the genotypes of 24 selected germplasm accessions. Among the 33 markers, 27 were successfully multiplexed and 23 had 100% SNP call rates. Results from analysis of "kompetitive allele-specific PCR" (KASP) and sequence tagged site (STS) markers developed from the same loci fully verified the genotype calls of 23 markers. The NGS-based multiplexed assay developed in this study is suitable for rapid and high-throughput screening of SNPs and some indel-based markers in wheat.
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